Compositions and methods for the treatment of asthma and allergy

ABSTRACT

The invention relates to the compounds of formula I or its pharmaceutical acceptable salts, as well as polymorphs, solvates, enantiomers, stereoisomers and hydrates thereof. The pharmaceutical compositions comprising an effective amount of compounds of formula I, and methods for the treatment of asthma and allergy may be formulated for oral, buccal, rectal, topical, transdermal, transmucosal, intravenous, parenteral administration, syrup, or injection. Such compositions may be used to treatment of respiratory diseases, respiratory disorders, COPD, bronchitis, brain injury, inflammation, inflammatory skin diseases, asthma, allergic reactions, infections due to acute allergy, bronchospasm, respiratory distress, acute asthma, leukotrienes over activity, 5-LO enzyme activity and cancer.

PRIORITY

The present application claims the benefit of Indian Provisional PatentApplication No. 1860/CHE/2012 filed on 10 May 2012 and the InternationalApplication No. PCT/IB2013/051561 filed on 27 Feb. 2013, the entiredisclosure of which is relied on for all purposes and is incorporatedinto this application by reference.

FIELD OF THE INVENTION

This disclosure generally relates to compounds and compositions for thetreatment of asthma, allergy and allergic rhinitis. More particularly,this invention relates to treating subjects with a pharmaceuticallyacceptable dose of compounds, crystals, esters, enantiomer,stereoisomer, salts, hydrates, prodrugs, or mixtures thereof.

BACKGROUND OF THE INVENTION

Asthma has consistently been reported as a major cause of chronic cough.The development of noninvasive assessment of airway inflammation led tothe identification of a condition that manifests chronic cough inindividuals without the abnormalities of airway function thatcharacterize asthma, but with sputum eosinophilia. This condition wasnamed nonasthmatic eosinophilic bronchitis (NAEB). The reason for theabsence of airway hyperresponsiveness in the NAEB remains unclear.Inflammation of the airways, with recruitment and activation of Tlymphocytes, eosinophils, and mast cells and release of inflammatorymediators, plays an important role in the pathophysiology of asthma andNAEB. Among lipid mediators, PGE2 is a mediator thought to have animportant role.

The accumulation of Eosinophilic bronchitis is a common cause of chroniccough, which like asthma is characterized by sputum eosinophilia, butunlike asthma there is no variable airflow obstruction or airwayhyperresponsiveness. Several studies suggest that prostaglandins mayplay an important role in orchestrating interactions between differentcells in several inflammatory diseases such as asthma. PGE2 is importantbecause of the multiplicity of its effects on immune response inrespiratory diseases; however, respiratory system appears to be uniquein that PGE2 has beneficial effects. The difference in airway functionobserved in patients with eosinophilic bronchitis and asthma could bedue to differences in PGE2 production. PGE2 present in induced sputumsupernatant from NAEB patients decreases BSMC proliferation, probablydue to simultaneous stimulation of EP2 and EP4 receptors with inhibitoryactivity. This protective effect of PGE2 may not only be the result of adirect action exerted on airway smooth-muscle proliferation but may alsobe attributable to the other anti-inflammatory actions.

Managing acute pathology of often relies on the addressing underlyingpathology and symptoms of the disease. There is currently a need in theart for new compositions to treatment of asthma and allergy.

SUMMARY OF THE INVENTION

The present invention provides compounds, compositions containing thesecompounds and methods for using the same to treat, prevent and/orameliorate the effects of the conditions such as asthma, allergy andallergic rhinitis.

The invention herein provides compositions comprising of formula I orpharmaceutical acceptable salts, hydrate, solvate, polymorphs, prodrug,enantiomer, or stereoisomer thereof. The invention also providespharmaceutical compositions comprising one or more compounds of formulaI or intermediates thereof and one or more of pharmaceuticallyacceptable carriers, vehicles or diluents. These compositions may beused in the treatment of asthma, allergy, allergic rhinitis and itsassociated complications.

In certain embodiments, the present invention relates to the compoundsand compositions of formula I, or pharmaceutically acceptable salts,hydrate, solvate, prodrug, polymorphs, enantiomer, or stereoisomerthereof,

Wherein,R¹ independently represents H, D, O, CD₃, OCH₃, OCD₃,

R² independently represents

a is independently 2, 3 or 7;

each b is independently 3, 5 or 6;

e is independently 1, 2 or 6;

c and d are each independently H, D, —OH, —OD, C₁-C₆-alkyl, —NH₂ or—COCH₃;

n is independently 1, 2, 3, 4 or 5.

In the illustrative embodiments, examples of compounds of formula I areas set forth below:

Herein the application also provides a kit comprising any of thepharmaceutical compositions disclosed herein. The kit may compriseinstructions for use in the treatment of asthma or its relatedcomplications.

The application also discloses a pharmaceutical composition comprising apharmaceutically acceptable carrier and any of the compositions herein.In some aspects, the pharmaceutical composition is formulated forsystemic administration, oral administration, sustained release,parenteral administration, injection, subdermal administration, ortransdermal administration.

Herein, the application additionally provides kits comprising thepharmaceutical compositions described herein. The kits may furthercomprise instructions for use in the treatment of asthma, allergy,allergic rhinitis or its related complications.

The compositions described herein have several uses. The presentapplication provides, for example, methods of treating a patientsuffering from asthma, allergy, allergic rhinitis or its relatedcomplications manifested from metabolic conditions, severe diseases ordisorders; Hepatology, Respiratory, Cancer, Hematological, Orthopedic,Cardiovascular, Renal, Skin, Neurological or Ocular complications.

DETAILED DESCRIPTION OF THE INVENTION Definitions

As used herein, the following terms and phrases shall have the meaningsset forth below. Unless defined otherwise, all technical and scientificterms used herein have the same meaning as commonly understood to one ofordinary skill in the art.

The compounds of the present invention can be present in the form ofpharmaceutically acceptable salts. The compounds of the presentinvention can also be present in the form of pharmaceutically acceptableesters (i.e., the methyl and ethyl esters of the acids of formula I tobe used as prodrugs). The compounds of the present invention can also besolvated, i.e. hydrated. The solvation can be affected in the course ofthe manufacturing process or can take place i.e. as a consequence ofhygroscopic properties of an initially anhydrous compound of formula I(hydration).

Compounds that have the same molecular formula but differ in the natureor sequence of bonding of their atoms or the arrangement of their atomsin space are termed “isomers.” Isomers that differ in the arrangement oftheir atoms in space are termed “stereoisomers.” Diastereomers arestereoisomers with opposite configuration at one or more chiral centerswhich are not enantiomers. Stereoisomers bearing one or more asymmetriccenters that are non-superimposable mirror images of each other aretermed “enantiomers.” When a compound has an asymmetric center, forexample, if a carbon atom is bonded to four different groups, a pair ofenantiomers is possible. An enantiomer can be characterized by theabsolute configuration of its asymmetric center or centers and isdescribed by the R- and S-sequencing rules of Cahn, Ingold and Prelog,or by the manner in which the molecule rotates the plane of polarizedlight and designated as dextrorotatory or levorotatory (i.e., as (+) or(−)-isomers respectively). A chiral compound can exist as eitherindividual enantiomer or as a mixture thereof. A mixture containingequal proportions of the enantiomers is called a “racemic mixture”.

Accordingly the compound of formula I represents a pharmacologicallyactive stereoisomer

In another aspect, the compound of formula I represents apharmacologically active stereoisomer

As used herein, the term “metabolic condition” refers to an Inbornerrors of metabolism (or genetic metabolic conditions) are geneticdisorders that result from a defect in one or more metabolic pathways;specifically, the function of an enzyme is affected and is eitherdeficient or completely absent.

The term “polymorph” as used herein is art-recognized and refers to onecrystal structure of a given compound.

The phrases “parenteral administration” and “administered parenterally”as used herein refer to modes of administration other than enteral andtopical administration, such as injections, and include withoutlimitation intravenous, intramuscular, intrapleural, intravascular,intrapericardial, intraarterial, intrathecal, intracapsular,intraorbital, intracardiac, intradennal, intraperitoneal, transtracheal,subcutaneous, subcuticular, intra-articular, subcapsular, subarachnoid,intraspinal and intrastemal injection and infusion.

A “patient,” “subject,” or “host” to be treated by the subject methodmay mean either a human or non-human animal, such as primates, mammals,and vertebrates.

The phrase “pharmaceutically acceptable” is art-recognized. In certainembodiments, the term includes compositions, polymers and othermaterials and/or dosage forms which are, within the scope of soundmedical judgment, suitable for use in contact with the tissues ofmammals, human beings and animals without excessive toxicity,irritation, allergic response, or other problem or complication,commensurate with a reasonable benefit/risk ratio.

The phrase “pharmaceutically acceptable carrier” is art-recognized, andincludes, for example, pharmaceutically acceptable materials,compositions or vehicles, such as a liquid or solid filler, diluent,solvent or encapsulating material involved in carrying or transportingany subject composition, from one organ, or portion of the body, toanother organ, or portion of the body. Each carrier must be “acceptable”in the sense of being compatible with the other ingredients of a subjectcomposition and not injurious to the patient. In certain embodiments, apharmaceutically acceptable carrier is non-pyrogenic. Some examples ofmaterials which may serve as pharmaceutically acceptable carriersinclude: (1) sugars, such as lactose, glucose and sucrose; (2) starches,such as corn starch and potato starch; (3) cellulose, and itsderivatives, such as sodium carboxymethyl cellulose, ethyl cellulose andcellulose acetate; (4) powdered tragacanth; (5) malt; (6) gelatin; (7)talc; (8) cocoa butter and suppository waxes; (9) oils, such as peanutoil, cottonseed oil, sunflower oil, sesame oil, olive oil, corn oil andsoybean oil; (10) glycols, such as propylene glycol; (11) polyols, suchas glycerin, sorbitol, mannitol and polyethylene glycol; (12) esters,such as ethyl oleate and ethyl laurate; (13) agar; (14) bufferingagents, such as magnesium hydroxide and aluminum hydroxide; (15) alginicacid; (16) pyrogen-free water; (17) isotonic saline; (18) Ringer'ssolution; (19) ethyl alcohol; (20) phosphate buffer solutions; and (21)other non-toxic compatible substances employed in pharmaceuticalformulations.

The term “prodrug” is intended to encompass compounds that, underphysiological conditions, are converted into the therapeutically activeagents of the present invention. A common method for making a prodrug isto include selected moieties that are hydrolyzed under physiologicalconditions to reveal the desired molecule. In other embodiments, theprodrug is converted by an enzymatic activity of the host animal.

The term “prophylactic or therapeutic” treatment is art-recognized andincludes administration to the host of one or more of the subjectcompositions. If it is administered prior to clinical manifestation ofthe unwanted condition (e.g., disease or other unwanted state of thehost animal) then the treatment is prophylactic, i.e., it protects thehost against developing the unwanted condition, whereas if it isadministered after manifestation of the unwanted condition, thetreatment is therapeutic, (i.e., it is intended to diminish, ameliorate,or stabilize the existing unwanted condition or side effects thereof).

The term “predicting” as used herein refers to assessing the probabilityrelated diseases patient will suffer from abnormalities or complicationand/or terminal platelet aggregation or failure and/or death (i.e.mortality) within a defined time window (predictive window) in thefuture. The mortality may be caused by the central nervous system orcomplication. The predictive window is an interval in which the subjectwill develop one or more of the said complications according to thepredicted probability. The predictive window may be the entire remaininglifespan of the subject upon analysis by the method of the presentinvention.

The term “treating” is art-recognized and includes preventing a disease,disorder or condition from occurring in an animal which may bepredisposed to the disease, disorder and/or condition but has not yetbeen diagnosed as having it; inhibiting the disease, disorder orcondition, e.g., impeding its progress; and relieving the disease,disorder, or condition, e.g., causing regression of the disease,disorder and/or condition. Treating the disease or condition includesameliorating at least one symptom of the particular disease orcondition, even if the underlying pathophysiology is not affected, suchas respiratory diseases, respiratory disorders, inflammation, asthma,allergy, bronchospasm, acute asthma, leukotrienes pathophysiology,cancer of a subject by administration of an agent even though such agentdoes not treat the cause of the condition. The term “treating”, “treat”or “treatment” as used herein includes curative, preventative (e.g.,prophylactic), adjunct and palliative treatment.

The phrase “therapeutically effective amount” is an art-recognized term.In certain embodiments, the term refers to an amount of a salt orcomposition disclosed herein that produces some desired effect at areasonable benefit/risk ratio applicable to any medical treatment. Incertain embodiments, the term refers to that amount necessary orsufficient to eliminate or reduce medical symptoms for a period of time.The effective amount may vary depending on such factors as the diseaseor condition being treated, the particular targeted constructs beingadministered, the size of the subject, or the severity of the disease orcondition. One of ordinary skill in the art may empirically determinethe effective amount of a particular composition without necessitatingundue experimentation.

In certain embodiments, the pharmaceutical compositions described hereinare formulated in a manner such that said compositions will be deliveredto a patient in a therapeutically effective amount, as part of aprophylactic or therapeutic treatment. The desired amount of thecomposition to be administered to a patient will depend on absorption,inactivation, and excretion rates of the drug as well as the deliveryrate of the salts and compositions from the subject compositions. It isto be noted that dosage values may also vary with the severity of thecondition to be alleviated. It is to be further understood that for anyparticular subject, specific dosage regimens should be adjusted overtime according to the individual need and the professional judgment ofthe person administering or supervising the administration of thecompositions. Typically, dosing will be determined using techniquesknown to one skilled in the art.

Additionally, the optimal concentration and/or quantities or amounts ofany particular salt or composition may be adjusted to accommodatevariations in the treatment parameters. Such treatment parametersinclude the clinical use to which the preparation is put, e.g., the sitetreated, the type of patient, e.g., human or non-human, adult or child,and the nature of the disease or condition.

In certain embodiments, the dosage of the subject compositions providedherein may be determined by reference to the plasma concentrations ofthe therapeutic composition or other encapsulated materials. Forexample, the maximum plasma concentration (Cmax) and the area under theplasma concentration-time curve from time 0 to infinity may be used.

When used with respect to a pharmaceutical composition or othermaterial, the term “sustained release” is art-recognized. For example, asubject composition which releases a substance over time may exhibitsustained release characteristics, in contrast to a bolus typeadministration in which the entire amount of the substance is madebiologically available at one time. For example, in particularembodiments, upon contact with body fluids including blood, spinalfluid, mucus secretions, lymph or the like, one or more of thepharmaceutically acceptable excipients may undergo gradual or delayeddegradation (e.g., through hydrolysis) with concomitant release of anymaterial incorporated therein, e.g., an therapeutic and/or biologicallyactive salt and/or composition, for a sustained or extended period (ascompared to the release from a bolus). This release may result inprolonged delivery of therapeutically effective amounts of any of thetherapeutic agents disclosed herein.

The phrases “systemic administration,” “administered systemically,”“peripheral administration” and “administered peripherally” areart-recognized, and include the administration of a subject composition,therapeutic or other material at a site remote from the disease beingtreated. Administration of an agent for the disease being treated, evenif the agent is subsequently distributed systemically, may be termed“local” or “topical” or “regional” administration, other than directlyinto the central nervous system, e.g., by subcutaneous administration,such that it enters the patient's system and, thus, is subject tometabolism and other like processes.

The phrase “therapeutically effective amount” is an art-recognized term.In certain embodiments, the term refers to an amount of a salt orcomposition disclosed herein that produces some desired effect at areasonable benefit/risk ratio applicable to any medical treatment. Incertain embodiments, the term refers to that amount necessary orsufficient to eliminate or reduce medical symptoms for a period of time.The effective amount may vary depending on such factors as the diseaseor condition being treated, the particular targeted constructs beingadministered, the size of the subject, or the severity of the disease orcondition. One of ordinary skill in the art may empirically determinethe effective amount of a particular composition without necessitatingundue experimentation.

The present disclosure also contemplates prodrugs of the compositionsdisclosed herein, as well as pharmaceutically acceptable salts of saidprodrugs.

This application also discloses a pharmaceutical composition comprisinga pharmaceutically acceptable carrier and the composition of a compoundof Formula I may be formulated for systemic or topical or oraladministration. The pharmaceutical composition may be also formulatedfor oral administration, oral solution, injection, subdermaladministration, or transdermal administration. The pharmaceuticalcomposition may further comprise at least one of a pharmaceuticallyacceptable stabilizer, diluent, surfactant, filler, binder, andlubricant.

In many embodiments, the pharmaceutical compositions described hereinwill incorporate the disclosed compounds and compositions (Formula I) tobe delivered in an amount sufficient to deliver to a patient atherapeutically effective amount of a compound of formula I orcomposition as part of a prophylactic or therapeutic treatment. Thedesired concentration of formula I or its pharmaceutical acceptablesalts will depend on absorption, inactivation, and excretion rates ofthe drug as well as the delivery rate of the salts and compositions fromthe subject compositions. It is to be noted that dosage values may alsovary with the severity of the condition to be alleviated. It is to befurther understood that for any particular subject, specific dosageregimens should be adjusted over time according to the individual needand the professional judgment of the person administering or supervisingthe administration of the compositions. Typically, dosing will bedetermined using techniques known to one skilled in the art.

Additionally, the optimal concentration and/or quantities or amounts ofany particular compound of formula I may be adjusted to accommodatevariations in the treatment parameters. Such treatment parametersinclude the clinical use to which the preparation is put, e.g., the sitetreated, the type of patient, e.g., human or non-human, adult or child,and the nature of the disease or condition.

The concentration and/or amount of any compound of formula I may bereadily identified by routine screening in animals, e.g., rats, byscreening a range of concentration and/or amounts of the material inquestion using appropriate assays. Known methods are also available toassay local tissue concentrations, diffusion rates of the salts orcompositions, and local blood flow before and after administration oftherapeutic formulations disclosed herein. One such method ismicrodialysis, as reviewed by T. E. Robinson et al., 1991, microdialysisin the neurosciences, Techniques, volume 7, Chapter 1. The methodsreviewed by Robinson may be applied, in brief, as follows. Amicrodialysis loop is placed in situ in a test animal. Dialysis fluid ispumped through the loop. When compounds with formula I such as thosedisclosed herein are injected adjacent to the loop, released drugs arecollected in the dialysate in proportion to their local tissueconcentrations. The progress of diffusion of the salts or compositionsmay be determined thereby with suitable calibration procedures usingknown concentrations of salts or compositions.

In certain embodiments, the dosage of the subject compounds of formula Iprovided herein may be determined by reference to the plasmaconcentrations of the therapeutic composition or other encapsulatedmaterials. For example, the maximum plasma concentration (Cmax) and thearea under the plasma concentration-time curve from time 0 to infinitymay be used.

Generally, in carrying out the methods detailed in this application, aneffective dosage for the compounds of Formulas I is in the range ofabout 0.01 mg/kg/day to about 100 mg/kg/day in single or divided doses,for instance 0.01 mg/kg/day to about 50 mg/kg/day in single or divideddoses. The compounds of Formulas I may be administered at a dose of, forexample, less than 0.2 mg/kg/day, 0.5 mg/kg/day, 1.0 mg/kg/day, 5mg/kg/day, 10 mg/kg/day, 20 mg/kg/day, 30 mg/kg/day, or 40 mg/kg/day.Compounds of Formula I may also be administered to a human patient at adose of, for example, between 0.1 mg and 1000 mg, between 5 mg and 80mg, or less than 1.0, 9.0, 12.0, 20.0, 50.0, 75.0, 100, 300, 400, 500,800, 1000, 2000, 5000 mg per day. In certain embodiments, thecompositions herein are administered at an amount that is less than 95%,90%, 80%, 70%, 60%, 50%, 40%, 30%, 20%, or 10% of the compound offormula I required for the same therapeutic benefit.

An effective amount of the compounds of formula I described hereinrefers to the amount of one of said salts or compositions which iscapable of inhibiting or preventing a disease.

An effective amount may be sufficient to prohibit, treat, alleviate,ameliorate, halt, restrain, slow or reverse the progression, or reducethe severity of a complication resulting from nerve damage ordemyelization and/or elevated reactive oxidative-nitrosative speciesand/or abnormalities in physiological homeostasis's, in patients who areat risk for such complications. As such, these methods include bothmedical therapeutic (acute) and/or prophylactic (prevention)administration as appropriate. The amount and timing of compositionsadministered will, of course, be dependent on the subject being treated,on the severity of the affliction, on the manner of administration andon the judgment of the prescribing physician. Thus, because ofpatient-to-patient variability, the dosages given above are a guidelineand the physician may titrate doses of the drug to achieve the treatmentthat the physician considers appropriate for the patient. In consideringthe degree of treatment desired, the physician must balance a variety offactors such as age of the patient, presence of preexisting disease, aswell as presence of other diseases.

The compositions provided by this application may be administered to asubject in need of treatment by a variety of conventional routes ofadministration, including orally, topically, parenterally, e.g.,intravenously, subcutaneously or intramedullary. Further, thecompositions may be administered intranasally, as a rectal suppository,or using a “flash” formulation, i.e., allowing the medication todissolve in the mouth without the need to use water. Furthermore, thecompositions may be administered to a subject in need of treatment bycontrolled release dosage forms, site specific drug delivery,transdermal drug delivery, patch (active/passive) mediated drugdelivery, by stereotactic injection, or in nanoparticles.

The compositions may be administered alone or in combination withpharmaceutically acceptable carriers, vehicles or diluents, in eithersingle or multiple doses. Suitable pharmaceutical carriers, vehicles anddiluents include inert solid diluents or fillers, sterile aqueoussolutions and various organic solvents. The pharmaceutical compositionsformed by combining the compositions and the pharmaceutically acceptablecarriers, vehicles or diluents are then readily administered in avariety of dosage forms such as tablets, powders, lozenges, syrups,injectable solutions and the like. These pharmaceutical compositionscan, if desired, contain additional ingredients such as flavorings,binders, excipients and the like. Thus, for purposes of oraladministration, tablets containing various excipients such asL-arginine, sodium citrate, calcium carbonate and calcium phosphate maybe employed along with various disintegrates such as starch, alginicacid and certain complex silicates, together with binding agents such aspolyvinylpyrrolidone, sucrose, gelatin and acacia. Additionally,lubricating agents such as magnesium stearate, sodium lauryl sulfate andtalc are often useful for tabletting purposes. Solid compositions of asimilar type may also be employed as fillers in soft and hard filledgelatin capsules. Appropriate materials for this include lactose or milksugar and high molecular weight polyethylene glycols. When aqueoussuspensions or elixirs are desired for oral administration, theessential active ingredient therein may be combined with varioussweetening or flavoring agents, coloring matter or dyes and, if desired,emulsifying or suspending agents, together with diluents such as water,ethanol, propylene glycol, glycerin and combinations thereof. Thecompounds of formula I may also comprise enterically coated comprisingof various excipients, as is well known in the pharmaceutical art.

For parenteral administration, solutions of the compositions may beprepared in (for example) sesame or peanut oil, aqueous propyleneglycol, or in sterile aqueous solutions may be employed. Such aqueoussolutions should be suitably buffered if necessary and the liquiddiluent first rendered isotonic with sufficient saline or glucose. Theseparticular aqueous solutions are especially suitable for intravenous,intramuscular, subcutaneous and intraperitoneal administration. In thisconnection, the sterile aqueous media employed are all readily availableby standard techniques known to those skilled in the art.

The formulations, for instance tablets, may contain e.g. 10 to 100, 50to 250, 150 to 500 mg, or 350 to 800 mg e.g. 10, 50, 100, 300, 500, 700,800 mg of the compounds of formula I disclosed herein, for instance,compounds of formula I or pharmaceutical acceptable salts of a compoundsof Formula I.

Generally, a composition as described herein may be administered orally,or parenterally (e.g., intravenous, intramuscular, subcutaneous orintramedullary). Topical administration may also be indicated, forexample, where the patient is suffering from gastrointestinal disorderthat prevent oral administration, or whenever the medication is bestapplied to the surface of a tissue or organ as determined by theattending physician. Localized administration may also be indicated, forexample, when a high dose is desired at the target tissue or organ. Forbuccal administration the active composition may take the form oftablets or lozenges formulated in a conventional manner.

The dosage administered will be dependent upon the identity of themetabolic disease; the type of host involved, including its age, healthand weight; the kind of concurrent treatment, if any; the frequency oftreatment and therapeutic ratio.

Illustratively, dosage levels of the administered active ingredientsare: intravenous, 0.1 to about 200 mg/kg; intramuscular, 1 to about 500mg/kg; orally, 5 to about 1000 mg/kg; intranasal instillation, 5 toabout 1000 mg/kg; and aerosol, 5 to about 1000 mg/kg of host bodyweight.

Expressed in terms of concentration, an active ingredient can be presentin the compositions of the present invention for localized use about thecutis, intranasally, pharyngolaryngeally, bronchially, intravaginally,rectally, or ocularly in a concentration of from about 0.01 to about 50%w/w of the composition; preferably about 1 to about 20% w/w of thecomposition; and for parenteral use in a concentration of from about0.05 to about 50% w/v of the composition and preferably from about 5 toabout 20% w/v.

The compositions of the present invention are preferably presented foradministration to humans and animals in unit dosage forms, such astablets, capsules, pills, powders, granules, suppositories, sterileparenteral solutions or suspensions, sterile non-parenteral solutions ofsuspensions, and oral solutions or suspensions and the like, containingsuitable quantities of an active ingredient. For oral administrationeither solid or fluid unit dosage forms can be prepared.

As discussed above, the tablet core contains one or more hydrophilicpolymers. Suitable hydrophilic polymers include, but are not limited to,water swellable cellulose derivatives, polyalkylene glycols,thermoplastic polyalkylene oxides, acrylic polymers, hydrocolloids,clays, gelling starches, swelling cross-linked polymers, and mixturesthereof. Examples of suitable water swellable cellulose derivativesinclude, but are not limited to, sodium carboxymethylcellulose,cross-linked hydroxypropylcellulose, hydroxypropyl cellulose (HPC),hydroxypropylmethylcellulose (HPMC), hydroxyisopropylcellulose,hydroxybutylcellulose, hydroxyphenylcellulose, hydroxyethylcellulose(HEC), hydroxypentylcellulose, hydroxypropylethylcellulose,hydroxypropylbutylcellulose, and hydroxypropylethylcellulose, andmixtures thereof. Examples of suitable polyalkylene glycols include, butare not limited to, polyethylene glycol. Examples of suitablethermoplastic polyalkylene oxides include, but are not limited to,poly(ethylene oxide). Examples of suitable acrylic polymers include, butare not limited to, potassium methacrylatedivinylbenzene copolymer,polymethylmethacrylate, high-molecular weight crosslinked acrylic acidhomopolymers and copolymers such as those commercially available fromNoveon Chemicals under the tradename CARBOPOL™. Examples of suitablehydrocolloids include, but are not limited to, alginates, agar, guargum, locust bean gum, kappa carrageenan, iota carrageenan, tara, gumarabic, tragacanth, pectin, xanthan gum, gellan gum, maltodextrin,galactomannan, pusstulan, laminarin, scleroglucan, gum arabic, inulin,pectin, gelatin, whelan, rhamsan, zooglan, methylan, chitin,cyclodextrin, chitosan, and mixtures thereof. Examples of suitable claysinclude, but are not limited to, smectites such as bentonite, kaolin,and laponite; magnesium trisilicate; magnesium aluminum silicate; andmixtures thereof. Examples of suitable gelling starches include, but arenot limited to, acid hydrolyzed starches, swelling starches such assodium starch glycolate and derivatives thereof, and mixtures thereof.Examples of suitable swelling cross-linked polymers include, but are notlimited to, cross-linked polyvinyl pyrrolidone, cross-linked agar, andcross-linked carboxymethylcellulose sodium, and mixtures thereof.

The carrier may contain one or more suitable excipients for theformulation of tablets. Examples of suitable excipients include, but arenot limited to, fillers, adsorbents, binders, disintegrants, lubricants,glidants, release-modifying excipients, superdisintegrants,antioxidants, and mixtures thereof.

Suitable binders include, but are not limited to, dry binders such aspolyvinyl pyrrolidone and hydroxypropylmethylcellulose; wet binders suchas water-soluble polymers, including hydrocolloids such as acacia,alginates, agar, guar gum, locust bean, carrageenan,carboxymethylcellulose, tara, gum arabic, tragacanth, pectin, xanthan,gellan, gelatin, maltodextrin, galactomannan, pusstulan, laminarin,scleroglucan, inulin, whelan, rhamsan, zooglan, methylan, chitin,cyclodextrin, chitosan, polyvinyl pyrrolidone, cellulosics, sucrose, andstarches; and mixtures thereof. Suitable disintegrants include, but arenot limited to, sodium starch glycolate, cross-linkedpolyvinylpyrrolidone, cross-linked carboxymethylcellulose, starches,microcrystalline cellulose, and mixtures thereof.

Suitable lubricants include, but are not limited to, long chain fattyacids and their salts, such as magnesium stearate and stearic acid,talc, glycerides waxes, and mixtures thereof. Suitable glidants include,but are not limited to, colloidal silicon dioxide. Suitablerelease-modifying excipients include, but are not limited to, insolubleedible materials, pH-dependent polymers, and mixtures thereof.

Suitable insoluble edible materials for use as release-modifyingexcipients include, but are not limited to, water-insoluble polymers andlow-melting hydrophobic materials, copolymers thereof, and mixturesthereof. Examples of suitable water-insoluble polymers include, but arenot limited to, ethylcellulose, polyvinyl alcohols, polyvinyl acetate,polycaprolactones, cellulose acetate and its derivatives, acrylates,methacrylates, acrylic acid copolymers, copolymers thereof, and mixturesthereof. Suitable low-melting hydrophobic materials include, but are notlimited to, fats, fatty acid esters, phospholipids, waxes, and mixturesthereof. Examples of suitable fats include, but are not limited to,hydrogenated vegetable oils such as for example cocoa butter,hydrogenated palm kernel oil, hydrogenated cottonseed oil, hydrogenatedsunflower oil, and hydrogenated soybean oil, free fatty acids and theirsalts, and mixtures thereof. Examples of suitable fatty acid estersinclude, but are not limited to, sucrose fatty acid esters, mono-, di-,and triglycerides, glyceryl behenate, glyceryl palmitostearate, glycerylmonostearate, glyceryl tristearate, glyceryl trilaurylate, glycerylmyristate, GlycoWax-932, lauroyl macrogol-32 glycerides, stearoylmacrogol-32 glycerides, and mixtures thereof. Examples of suitablephospholipids include phosphotidyl choline, phosphotidyl serene,phosphotidyl enositol, phosphotidic acid, and mixtures thereof. Examplesof suitable waxes include, but are not limited to, carnauba wax,spermaceti wax, beeswax, candelilla wax, shellac wax, microcrystallinewax, and paraffin wax; fat-containing mixtures such as chocolate, andmixtures thereof. Examples of super disintegrants include, but are notlimited to, croscarmellose sodium, sodium starch glycolate andcross-linked povidone (crospovidone). In one embodiment the tablet corecontains up to about 5 percent by weight of such super disintegrant.

Examples of antioxidants include, but are not limited to, tocopherols,ascorbic acid, sodium pyrosulfite, butylhydroxytoluene, butylatedhydroxyanisole, edetic acid, and edetate salts, and mixtures thereof.Examples of preservatives include, but are not limited to, citric acid,tartaric acid, lactic acid, malic acid, acetic acid, benzoic acid, andsorbic acid, and mixtures thereof.

In one embodiment, the immediate release coating has an averagethickness of at least 50 microns, such as from about 50 microns to about2500 microns; e.g., from about 250 microns to about 1000 microns. Inembodiment, the immediate release coating is typically compressed at adensity of more than about 0.9 g/cc, as measured by the weight andvolume of that specific layer.

In one embodiment, the immediate release coating contains a firstportion and a second portion, wherein at least one of the portionscontains the second pharmaceutically active agent. In one embodiment,the portions contact each other at a center axis of the tablet. In oneembodiment, the first portion includes the first pharmaceutically activeagent and the second portion includes the second pharmaceutically activeagent.

In one embodiment, the first portion contains the first pharmaceuticallyactive agent and the second portion contains the second pharmaceuticallyactive agent. In one embodiment, one of the portions contains a thirdpharmaceutically active agent. In one embodiment one of the portionscontains a second immediate release portion of the same pharmaceuticallyactive agent as that contained in the tablet core.

In one embodiment, the outer coating portion is prepared as a dry blendof materials prior to addition to the coated tablet core. In anotherembodiment the outer coating portion is included of a dried granulationincluding the pharmaceutically active agent.

Formulations with different drug release mechanisms described abovecould be combined in a final dosage form containing single or multipleunits. Examples of multiple units include multilayer tablets, capsulescontaining tablets, beads, or granules in a solid or liquid form.Typical, immediate release formulations include compressed tablets,gels, films, coatings, liquids and particles that can be encapsulated,for example, in a gelatin capsule. Many methods for preparing coatings,covering or incorporating drugs, are known in the art.

The immediate release dosage, unit of the dosage form, i.e., a tablet, aplurality of drug-containing beads, granules or particles, or an outerlayer of a coated core dosage form, contains a therapeutically effectivequantity of the active agent with conventional pharmaceuticalexcipients. The immediate release dosage unit may or may not be coated,and may or may not be admixed with the delayed release dosage unit orunits (as in an encapsulated mixture of immediate releasedrug-containing granules, particles or beads and delayed releasedrug-containing granules or beads).

Extended release formulations are generally prepared as diffusion orosmotic systems, for example, as described in “Remington—The Science andPractice of Pharmacy”, 20th. Ed., Lippincott Williams & Wilkins,Baltimore, Md., 2000). A diffusion system typically consists of one oftwo types of devices, reservoir and matrix, which are wellknown anddescribed in die art. The matrix devices are generally prepared bycompressing the drug with a slowly dissolving polymer carrier into atablet form.

An immediate release portion can be added to the extended release systemby means of either applying an immediate release layer on top of theextended release core; using coating or compression processes or in amultiple unit system such as a capsule containing extended and immediaterelease beads.

Delayed release dosage formulations are created by coating a soliddosage form with a film of a polymer which is insoluble in the acidenvironment of the stomach, but soluble in the neutral environment ofsmall intestines. The delayed release dosage units can be prepared, forexample, by coating a drug or a drug-containing composition with aselected coating material. The drug-containing composition may be atablet for incorporation into a capsule, a tablet for use as an innercore in a “coated core” dosage form, or a plurality of drug-containingbeads, particles or granules, for incorporation into either a tablet orcapsule.

A pulsed release dosage form is one that mimics a multiple dosingprofile without repeated dosing and typically allows at least a twofoldreduction in dosing frequency as compared to the drug presented as aconventional dosage form (e.g., as a solution or prompt drug-releasing,conventional solid dosage form). A pulsed release profile ischaracterized by a time period of no release (lag time) or reducedrelease followed by rapid drug release.

Each dosage form contains a therapeutically effective amount of activeagent. In one embodiment of dosage forms that mimic a twice daily dosingprofile, approximately 30 wt. % to 70 wt. %, preferably 40 wt. % to 60wt. %, of the total amount of active agent in the dosage form isreleased in the initial pulse, and, correspondingly approximately 70 wt.% to 3.0 wt. %, preferably 60 wt. % to 40 wt. %, of the total amount ofactive agent in the dosage form is released in the second pulse. Fordosage forms mimicking the twice daily dosing profile, the second pulseis preferably released approximately 3 hours to less than 14 hours, andmore preferably approximately 5 hours to 12 hours, followingadministration.

Another dosage form contains a compressed tablet or a capsule having adrug-containing immediate release dosage unit, a delayed release dosageunit and an optional second delayed release dosage unit. In this dosageform, the immediate release dosage unit contains a plurality of beads,granules particles that release drug substantially immediately followingoral administration to provide an initial dose. The delayed releasedosage unit contains a plurality of coated beads or granules, whichrelease drug approximately 3 hours to 14 hours following oraladministration to provide a second dose.

For purposes of transdermal (e.g., topical) administration, dilutesterile, aqueous or partially aqueous solutions (usually in about 0.1%to 5% concentration), otherwise similar to the above parenteralsolutions, may be prepared.

Methods of preparing various pharmaceutical compositions with a certainamount of one or more compounds of formula I or other active agents areknown, or will be apparent in light of this disclosure, to those skilledin this art. For examples of methods of preparing pharmaceuticalcompositions, see Remington's Pharmaceutical Sciences, Mack PublishingCompany, Easton, Pa., 19th Edition (1995).

In addition, in certain embodiments, subject compositions of the presentapplication maybe lyophilized or subjected to another appropriate dryingtechnique such as spray drying. The subject compositions may beadministered once, or may be divided into a number of smaller doses tobe administered at varying intervals of time, depending in part on therelease rate of the compositions and the desired dosage.

Formulations useful in the methods provided herein include thosesuitable for oral, nasal, topical (including buccal and sublingual),rectal, vaginal, aerosol and/or parenteral administration. Theformulations may conveniently be presented in unit dosage form and maybe prepared by any methods well known in the art of pharmacy. The amountof a subject composition which may be combined with a carrier materialto produce a single dose may vary depending upon the subject beingtreated, and the particular mode of administration.

Methods of preparing these formulations or compositions include the stepof bringing into association subject compositions with the carrier and,optionally, one or more accessory ingredients. In general, theformulations are prepared by uniformly and intimately bringing intoassociation a subject composition with liquid carriers, or finelydivided solid carriers, or both, and then, if necessary, shaping theproduct.

The compounds of formula I described herein may be administered ininhalant or aerosol formulations. The inhalant or aerosol formulationsmay comprise one or more agents, such as adjuvants, diagnostic agents,imaging agents, or therapeutic agents useful in inhalation therapy. Thefinal aerosol formulation may for example contain 0.005-90% w/w, forinstance 0.005-50%, 0.005-5% w/w, or 0.01-1.0% w/w, of medicamentrelative to the total weight of the formulation.

In solid dosage forms for oral administration (capsules, tablets, pills,dragees, powders, granules and the like), the subject composition ismixed with one or more pharmaceutically acceptable carriers and/or anyof the following: (1) fillers or extenders, such as starches, lactose,sucrose, glucose, mannitol, and/or silicic acid; (2) binders, such as,for example, carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidone, sucrose and/or acacia; (3) humectants, such as glycerol;(4) disintegrating agents, such as agar-agar, calcium carbonate, potatoor tapioca starch, alginic acid, certain silicates, and sodiumcarbonate; (5) solution retarding agents, such as paraffin; (6)absorption accelerators, such as quaternary ammonium compounds; (7)wetting agents, such as, for example, acetyl alcohol and glycerolmonostearate; (8) absorbents, such as kaolin and bentonite clay; (9)lubricants, such a talc, calcium stearate, magnesium stearate, solidpolyethylene glycols, sodium lauryl sulfate, and mixtures thereof; and(10) coloring agents. In the case of capsules, tablets and pills, thepharmaceutical compositions may also comprise buffering agents. Solidcompositions of a similar type may also be employed as fillers in softand hard-filled gelatin capsules using lactose or milk sugars, as wellas high molecular weight polyethylene glycols and the like.

Liquid dosage forms for oral administration include pharmaceuticallyacceptable emulsions, microemulsions, solutions, suspensions, syrups andelixirs. In addition to the subject compositions, the liquid dosageforms may contain inert diluents commonly used in the art, such as, forexample, water or other solvents, solubilizing agents and emulsifiers,such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethylacetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butyleneglycol, oils (in particular, cottonseed, corn, peanut, sunflower,soybean, olive, castor, and sesame oils), glycerol, tetrahydrofurylalcohol, polyethylene glycols and fatty acid esters of sorbitan, andmixtures thereof.

Suspensions, in addition to the subject compositions, may containsuspending agents such as, for example, ethoxylated isostearyl alcohols,polyoxyethylene sorbitol, and sorbitan esters, microcrystallinecellulose, aluminum metahydroxide, bentonite, agar-agar and tragacanth,and mixtures thereof.

Formulations for rectal or vaginal administration may be presented as asuppository, which may be prepared by mixing a subject composition withone or more suitable non-irritating carriers comprising, for example,cocoa butter, polyethylene glycol, a suppository wax, or a salicylate,and which is solid at room temperature, but liquid at body temperatureand, therefore, will melt in the appropriate body cavity and release theencapsulated compound(s) and composition(s). Formulations which aresuitable for vaginal administration also include pessaries, tampons,creams, gels, pastes, foams, or spray formulations containing suchcarriers as are known in the art to be appropriate.

Dosage forms for transdermal administration include powders, sprays,ointments, pastes, creams, lotions, gels, solutions, patches, andinhalants. A subject composition may be mixed under sterile conditionswith a pharmaceutically acceptable carrier, and with any preservatives,buffers, or propellants that may be required. For transdermaladministration, the complexes may include lipophilic and hydrophilicgroups to achieve the desired water solubility and transport properties.

The ointments, pastes, creams and gels may contain, in addition tosubject compositions, other carriers, such as animal and vegetable fats,oils, waxes, paraffins, starch, tragacanth, cellulose derivatives,polyethylene glycols, silicones, bentonites, silicic acid, talc and zincoxide, or mixtures thereof. Powders and sprays may contain, in additionto a subject composition, excipients such as lactose, talc, silicicacid, aluminum hydroxide, calcium silicates and polyamide powder, ormixtures of such substances. Sprays may additionally contain customarypropellants, such as chlorofluorohydrocarbons and volatile unsubstitutedhydrocarbons, such as butane and propane.

Methods of delivering a composition or compositions via a transdermalpatch are known in the art. Exemplary patches and methods of patchdelivery are described in U.S. Pat. Nos. 6,974,588, 6,564,093,6,312,716, 6,440,454, 6,267,983, 6,239,180, and 6,103,275.

In another embodiment, a transdermal patch may comprise: a substratesheet comprising a composite film formed of a resin compositioncomprising 100 parts by weight of a polyvinyl chloride-polyurethanecomposite and 2-10 parts by weight of astyrene-ethylene-butylene-styrene copolymer, a first adhesive layer onthe one side of the composite film, and a polyalkylene terephthalatefilm adhered to the one side of the composite film by means of the firstadhesive layer, a primer layer which comprises a saturated polyesterresin and is formed on the surface of the polyalkylene terephthalatefilm; and a second adhesive layer comprising a styrene-diene-styreneblock copolymer containing a pharmaceutical agent layered on the primerlayer. A method for the manufacture of the above-mentioned substratesheet comprises preparing the above resin composition molding the resincomposition into a composite film by a calendar process, and thenadhering a polyalkylene terephthalate film on one side of the compositefilm by means of an adhesive layer thereby forming the substrate sheet,and forming a primer layer comprising a saturated polyester resin on theouter surface of the polyalkylene terephthalate film.

Another type of patch comprises incorporating the drug directly in apharmaceutically acceptable adhesive and laminating the drug-containingadhesive onto a suitable backing member, e.g. a polyester backingmembrane. The drug should be present at a concentration which will notaffect the adhesive properties, and at the same time deliver therequired clinical dose.

Transdermal patches may be passive or active. Passive transdermal drugdelivery systems currently available, such as the nicotine, estrogen andnitroglycerine patches, deliver small-molecule drugs. Many of the newlydeveloped proteins and peptide drugs are too large to be deliveredthrough passive transdermal patches and may be delivered usingtechnology such as electrical assist (iontophoresis) for large-moleculedrugs.

Iontophoresis is a technique employed for enhancing the flux of ionizedsubstances through membranes by application of electric current. Oneexample of an iontophoretic membrane is given in U.S. Pat. No. 5,080,646to Theeuwes. The principal mechanisms by which iontophoresis enhancesmolecular transport across the skin are (a) repelling a charged ion froman electrode of the same charge, (b) electroosmosis, the convectivemovement of solvent that occurs through a charged pore in response thepreferential passage of counter-ions when an electric field is appliedor (c) increase skin permeability due to application of electricalcurrent.

In some cases, it may be desirable to administer in the form of a kit,it may comprise a container for containing the separate compositionssuch as a divided bottle or a divided foil packet. Typically the kitcomprises directions for the administration of the separate components.The kit form is particularly advantageous when the separate componentsare preferably administered in different dosage forms (e.g., oral andparenteral), are administered at different dosage intervals, or whentitration of the individual components of the combination is desired bythe prescribing physician.

An example of such a kit is a so-called blister pack. Blister packs arewell known in the packaging industry and are widely used for thepackaging of pharmaceutical unit dosage forms (tablets, capsules, andthe like). Blister packs generally consist of a sheet of relativelystiff material covered with a foil of a plastic material that may betransparent.

Methods and compositions for the treatment of asthma, allergy, allergicrhinitis. Among other things, herein is provided a method of treatingAsthma, allergy, allergic rhinitis, comprising administering to apatient in need thereof a therapeutically effective amount of compoundof Formula I:

Wherein,

R¹ independently represents H, D, O, CD₃, OCH₃, OCD₃,

R² independently represents

a is independently 2, 3 or 7;

each b is independently 3, 5 or 6;

e is independently 1, 2 or 6;

c and d are each independently H, D, —OH, —OD, C₁-C₆-alkyl, —NH₂ or—COCH₃;

n is independently 1, 2, 3, 4 or 5.

Methods for Using Compounds of Formula I:

The invention also includes methods for treating asthma and allergyincluding respiratory diseases, respiratory disorders, COPD, bronchitis,brain injury, inflammation, asthma, allergy, bronchospasm, respiratorydistress, acute asthma, leukotrienes over activity, 5-LO enzymeactivity, cancer.

Methods of Making

Examples of synthetic pathways useful for making compounds of formula Iare set forth in example below and generalized in scheme 1:

Step-1: Synthesis of Compound 3:

A solution of 9.78 g (60 mmol) of 2-ethylbenzo[b]thiophene 1 in 10 ml ofheptane was added, over 10 minutes, to a mixture of 9.43 g (33 mmol) of1,3-dibromo-5,5-dimethylhydantoin 2 and 0.49 g (3 mmol) ofazobisisobutyronitrile in 117.5 ml of heptane preheated to 60° C. Themixture was maintained for 1 additional hour at this temperature. Aftercooling to 20° C., stirring was continued for 1 hour and then the5,5-dimethylhydantoin which has precipitated was filtered off and washedwith 10 ml of heptane. The filtrate was washed with an aqueous sodiumthiosulphate solution (3 g/100 ml) and then with 3 times 100 ml ofwater. After drying over sodium sulphate, the heptane phase wasconcentrated to approximately 40 ml and then cooled to −10° C. for onehour and a half. The precipitate formed was filtered off and dried underpartial vacuum at 20° C. to provide 9.05 g of the desired compound inthe form of a beige powder, which represents a yield of 57% (M.P.: 53°C., purity by liquid phase chromatography: 92%). A second, less puresample was obtained by concentrating the mother liquors (16%),2-(1-bromoethyl)benzo[b]thiophene was obtained with a yield of 73%.

Step-2: Synthesis of Compound 5:

1 g (4 mmol) of compound 3 (purity: 97%) and 1.48 g (12 mmol) ofO-benzylhydroxylamine 4 are dissolved, under a nitrogen atmosphere, in 2ml of anhydrous tetrahydrofuran. The mixture was stirred for 5.5 hoursat 20° C. After addition of 15 ml of water, the reaction mixture wasacidified to pH=3 with dilute hydrochloric acid and extraction werecarried out with 4 times 15 ml of diethyl ether. The ether phase wasdried over sodium sulphate and concentrated under reduced pressure,which gives 1.44 g of brown oil. Filtration was then carried out througha silica gel column (eluent: 1/99 to 30/70 gradient of dichloromethanein hexane), 0.89 g of compound 5 was obtained in the form of apink-beige solid. M.P.: 55°-56° C. Yield: 76%.

Step-3: Synthesis of Compound 7:

10.1 g (33.6 mmol) of compound 5 (purity approximately 94%) and 12.5 g(3.3 mol equiv) of trimethylsilyl isocyanate 6 are dissolved in 25 ml oftetrahydrofuran. The mixture was heated at reflux for 48 hours. Aftercooling to 25° C., 150 ml of a saturated aqueous ammonium chloridesolution are added, stirring was carried out for 1 hour and the mixturewas extracted with two times 50 ml of ethyl acetate. The organic phasesare combined and washed with two times 25 ml of water. The combinedorganic phases are dried over sodium sulphate and evaporated to drynessand the residue was purified by silica gel chromatography. In this way,5.9 g of compound 7 was obtained in the form of a cream powder. M.P.:126° C. Yield: 54%.

Step-4: Synthesis of Compound 10:

3.25 g of sodium are dissolved in portions in 300 ml of ethanol withstirring. A solution of 4.3 g of 2,6-dihydroxyacetophenone 8 and 15.5 mlof diethyl oxalate 9 in 25 ml of ethanol was subsequently added dropwise. The reaction mixture was subsequently heated at 80° for 3 hours.The mixture was cooled to room temperature, and 10 ml of 32% HCl areadded drop wise. The mixture was heated at 90° for 30 minutes andcooled, and the solvent was removed and 5.9 g of compound 10 wasobtained.

Step-5: Synthesis of Compound 11:

A solution of 2.0 g of compound 10 in 30 ml of acetic acid and 20 ml of32% HCl was heated under reflux for 2 h. The mixture was cooled, pouredonto ice and filtered, and the product was recrystallwased from ethanol,giving 1.5 g of compound 11.

Step-6: Synthesis of Compound 12:

0.46 ml of oxalyl chloride was added to a solution of 560 mg of compound11 in 15 ml of dichloromethane and 0.5 ml of DMF, and the mixture wasrefluxed for 1 hour. The solvents are then removed and the crude acidchloride 12 was used for next step without further purification.

Step-7: Synthesis of Compound 13:

Compound 7 (0.4 g, 1.0 mmol) in 2.5 mL of CH₂Cl₂ and 2.5 mL of CH₃CN wascooled to 0° C. Lithium t-butoxide (1.0 M in hexanes, 1.1 mL, 1.1 mmol)was added and the mixture was stirred at 0° C. for 15 min and then at RTfor 10 min. The mixture was re-cooled to 0° C. and compound 12 (1.2mmol) was added dropwise. The mixture was stirred for 10 min at 0° C.and then allowed to stir at RT overnight. The solution was diluted withCH2C12 and water and the layers are separated. The organic layer waswashed with water, brine, dried over Na2SO4, and cone in vacuo.Purification by silica gel chromatography afforded compound 13 with ayield of 78%.

Step-8: Synthesis of Compound 14:

6 mmol of compound 13 (purity approximately 94%), 1 g of 10%palladium-on-charcoal, 62.5 ml of glacial acetic acid and 6 drops of 12Nhydrochloric acid are introduced into a reactor (par flask). The mixturewas maintained for 24 hours at 50° C. under a hydrogen pressure of 5bar. After cooling, filtering off the catalyst through diatomaceousearth, neutralizing with sodium hydroxide, extracting with ethyl acetateand evaporating the solvent, the residue was purified by silica gelchromatography to obtain compound 14 with a yield of 64.9%. Mol. Wt.:424.07; Elemental Analysis: C, 59.43; H, 3.80; N, 6.60; 0, 22.62; S,7.551.

Examples Evaluation of Zileuton and Formula I (1-1) IntracolonicAdministration in Rat Model of Chronic Colitis

Female virgin Sprague-Dawley rats weighing 200-250 g were used in thisstudy. The animals were maintained in a restricted access room withcontrolled temperature (23° C.) and light/dark cycle (16 h:8 h). Therats were housed in individual isolated rack mounted wire cages.

TNB/ethanol colitis was induced in 90 rats. Animals were thereafterrandomised into four therapeutic groups to receive daily, from day 1 (24hours after induction of colitis):

Group A (n=30)−0.25 ml of vehicle solution enema (1-5%carboxymethylcellulose in saline serum) (placebo group).

Group B (n=30)−0.25 ml of the vehicle solution enema added with 50 mg/kgof body weight of 5-ASA.

Group C (n=30)−0-25 ml of the vehicle solution enema added with 50 mg/kgof body weight of zileuton.

Group D (n=30)−0-25 ml of the vehicle solution enema added with 50 mg/kgof body weight of Formula I (1-1) equivalent of zileuton.

In addition, sham colitis was induced, by intrarectal administration of0-25 ml of 0.9°/0 saline, in 10 rats (control group). At day 1 and 3,and at weeks 1, 2, and 4, 10 rats from groups A, B, C and D wererandomly selected for the assessment of eicosanoid release in the lumenof the colon by intracolonic dialysis. Rats were anaesthetised with 100mg of intraperitoneal thiopental and intracolonic dialysis was performedusing hydrated Visking seamless cellulose tubing (8/32, 6-3 mm diameter,7 cm long; Medicell International, London) attached by a 10 cmpolyurethane cannula to an external syringe. After inserting the entirecannula into the distal colon, the dialysis bag was filled with 1 ml ofdialysis solution, consisting of 0.3°/o bovine serum albumin in asolution of 120 mmol/1 NaCl and 30 mmol/1 KHCO3 adjusted to pH 7.90. Onehour later, the fluid was withdrawn and immediately stored at −30 C. Thevolume of the dialysate recovered at the end of the one hour period washigher than 90%. In the control group (n=10), an intracolonic dialysiswas performed in the same way 24 hours after the sham colitis induction.The day after the dialysis was performed at weeks 1, 2, and 4, the sameanimals were given a distal colectomy under total anaesthesia with 100mg of intraperitoneal thiopental, to assess colonic inflammationmacroscopically and histologically. The excised colon was openedlongitudinally, rinsed with normal saline, pinned out on a wax block,and assigned a code number. Mucosal damage was assessed macroscopicallyas described later. Afterwards, three tissue specimens (2×10 mm) wereobtained from the colon. When no severely visible inflammation waspresent, the specimens were taken from the regions 1 cm, 3 cm, and 8 cmproximal to the anus. When visible lesions were present, the specimenswere taken from the affected regions. Tissue samples were fixed informaldehyde and routinely processed. In the control group (n=10) therats were killed in the same way 48 hours after induction of shamcolitis.

Effects of Treatment on Macroscopic Colonic Damage:

As previously described, intracolonic administration of TNB/ethanolresulted in extensive ulceration and transmural inflammation of thedistal colon with severe thickening of the bowel wall and strictures. Inaddition, segmental pericolonic accumulations of mesenteric fat andfibrinous adhesions to the small bowel were frequently seen. Themacroscopic damage score evaluated at weeks 1 and 2 after the colonicinjury was similar in the four groups studied. Formula I (1-1) treatedrats, however, showed a significant reduction in the macroscopic damagescore after four weeks of treatment compared with 5-ASA and zileuton(4.36 (0.6) v 7.3 (0.7), and 5.6 (0.7), respectively; p=0.026). Allparameters measured by the score improved in Formula I (1-1) group atfour weeks compared with 5-ASA, zileuton and placebo, mainly thedevelopment of strictures.

In summary, this study suggests that chronic intracolonic administrationof Formula I (1-1) a selective 5-lipoxygenase inhibitor and apolyunsaturated fatty acid, EPA, may improve the course of the disease,when compared with 5-ASA, Zileuton and placebo. This effect may berelated to an increased and maintained production of PGE2, reducedinflammatory factors together with the inhibition of the synthesis ofLTB4.

The term “sample” refers to a sample of a body fluid, to a sample ofseparated cells or to a sample from a tissue or an organ. Samples ofbody fluids can be obtained by well known techniques and include,preferably, samples of blood, plasma, serum, or urine, more preferably,samples of blood, plasma or serum. Tissue or organ samples may beobtained from any tissue or organ by, e.g., biopsy. Separated cells maybe obtained from the body fluids or the tissues or organs by separatingtechniques such as centrifugation or cell sorting. Preferably, cell-,tissue- or organ samples are obtained from those cells, tissues ororgans which express or produce the peptides referred to herein.

EQUIVALENTS

The present disclosure provides among other things compositions andmethods for treating asthma, allergy, allergic rhinitis and theircomplications. While specific embodiments of the subject disclosure havebeen discussed, the above specification was illustrative and notrestrictive. Many variations of the systems and methods herein willbecome apparent to those skilled in the art upon review of thisspecification. The full scope of the claimed systems and methods shouldbe determined by reference to the claims, along with their full scope ofequivalents, and the specification, along with such variations.

INCORPORATION BY REFERENCE

All publications and patents mentioned herein, including those itemslisted above, are hereby incorporated by reference in their entirety asif each individual publication or patent was specifically andindividually indicated to be incorporated by reference. In case ofconflict, the present application, including any definitions herein,will control.

The invention claimed is:
 1. A compound of Formula I:

or a pharmaceutically acceptable salt, hydrate, solvate, enantiomer, orstereoisomer thereof, wherein: R₁ represents

R₂ represents

a is 2, 3 or 7; each b is independently 3, 5 or 6; e is 1, 2 or 6; c andd are each independently H, D, —OH, —OD, C₁-C₆-alkyl, —NH₂ or —COCH₃;and n is 1, 2, 3, 4 or
 5. 2. A pharmaceutical composition comprising acompound of claim 1 and a pharmaceutically acceptable carrier.
 3. Thepharmaceutical composition of claim 2, further comprising a molecularconjugate of zileuton and a carboxylic acid compound selected from thegroup consisting of R-Lipoic acid, eicosapentaenoic acid,docosahexaenoic acid, salsalate, cromoglicic acid and fumaric acid. 4.The pharmaceutical composition of claim 3, wherein the carboxylic acidcompound is R-Lipoic acid.
 5. The pharmaceutical composition of claim 3,wherein the carboxylic acid compound is eicosapentaenoic acid.
 6. Thepharmaceutical composition of claim 3, wherein the carboxylic acidcompound is docosahexaenoic acid.
 7. The pharmaceutical composition ofclaim 3, wherein the carboxylic acid compound is salsalate.
 8. Thepharmaceutical composition of claim 3, wherein the carboxylic acidcompound is cromoglicic acid.
 9. The pharmaceutical composition of claim3, wherein the carboxylic acid compound is fumaric acid.